State
73,388 recalls have nationwide distribution and so reach Connecticut. 6,572 additional recalls listed Connecticut specifically in their distribution scope.
Of the 6,572 recalls naming Connecticut we have scored against our rubric, 838 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,881 (29%) are Severe.
Which agencies issued them
These figures cover only the 6,572 recalls whose distribution notice names Connecticut specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mack Trucks is recalling one 2021 LR Electric truck because a coolant line may not be fully seated, creating a risk of electrical short circuit and fire.
EZ Noble Sushi is recalling shrimp tempura and lobster roll products with expiration date 08/12/2022 distributed in Massachusetts and Connecticut due to undeclared wheat allergen.
Vi-Jon is recalling SWAN Citroma Magnesium Citrate Saline Laxative (10 FL OZ bottles) due to microbial contamination of a non-sterile product. The product was distributed nationwide in the USA, Canada, and Panama.
Dexter Axle is recalling Smart-Steer 2.0 self-steering axles because the steering arm may fracture, potentially causing a crash.
EZ Noble Sushi is recalling Pink Lady and Salmon Avocado rolls (9 oz, expiration 08/12/2022) distributed in MA and CT due to undeclared egg. Consumers with egg allergies should not consume this product.
Vi-Jon's CITROMA magnesium citrate laxative is recalled due to microbial contamination. Approximately 18,588 bottles were distributed nationwide in the USA, Canada, and Panama.
EZ Noble Sushi recalls spicy salmon rolls (9.6 oz, expiration 08/12/2022) sold in MA and CT due to undeclared egg allergen.
EZ Noble Sushi is recalling California crunch roll products due to undeclared wheat allergen. Consumers with wheat allergies should discard this product.
Equate Magnesium Citrate saline laxative has been recalled for microbial contamination. The FDA Class I recall affects 18,324 bottles distributed in the US, Canada, and Panama.
EZ Noble Sushi is recalling Spicy Tuna Roll (9.6 oz) with expiration 08/12/2022 due to undeclared egg. Consumers with egg allergies should not consume this product.
Carolina Infusion's QUAD-MIX 30/2/60/0.15 injectable (Lot 08022022@12) is recalled nationwide because the manufacturer failed to assure sterility. Patients and healthcare providers should not use affected vials and should contact the manufacturer.
Carolina Infusion is recalling TRI-MIX 30/2/40 Injectable because the manufacturer cannot assure the product's sterility. Non-sterile injectable drugs pose serious infection risks.
Exactech's GXL acetabular hip implant liners are being recalled because they were packaged in non-conforming bags that may cause accelerated wear of the devices.
Skinny Guy Campers is recalling Model 6.5 Campers because cracked quick disconnect fittings in the LP gas system may cause a gas leak, increasing fire risk.
Exactech GXL acetabular hip implant liners may have been packaged in non-conforming bags, which could contribute to accelerated device wear. Approximately 17,929 units were distributed worldwide.
SCENARIA View imaging software errors prevent image reconstruction, which may require additional scans and expose patients to unnecessary radiation.
Carolina Infusion is recalling MIC/B12 injectable vials due to lack of assurance of sterility. Affected lots were distributed nationwide.
Exactech recalls GXL acetabular hip implant liners packaged in non-conforming bags that may cause premature wear. No injuries have been reported.
EZ Noble Sushi is recalling Philadelphia avocado and cucumber classic rolls (8 oz) with expiration 08/12/2022 due to undeclared milk. The rolls were distributed in Massachusetts and Connecticut.
Carolina Infusion is recalling Sermorelin Acetate injectable (1 MG/ML, 9 ML syringes) distributed nationwide due to lack of assurance of sterility. The manufacturer could not adequately document that the product meets required sterility standards.
A software issue in the ZAP-X Radiosurgery System may cause incorrect treatment positioning in patients with large rotational deviations. The alignment algorithm could miscalculate treatment table offset values, potentially affecting treatment delivery.
Teva Pharmaceuticals is recalling 83,703 bottles of prescription amphetamine tablets nationwide because bottles labeled as 15 mg strength actually contain 20 mg tablets, creating risk of unintended overdose. Patients should contact their pharmacy or healthcare provider.
Exactech recalled 132 GXL acetabular liners (hip implant components) due to non-conforming bags that may accelerate device wear. Units were distributed worldwide to the US and 13 countries.
ICU Medical is recalling 5.8 million Trifuse Extension Sets due to a manufacturing defect that creates a visible gap between the connector's housing parts. The gap could lead to disconnection or fluid leakage during infusion.
Cook Incorporated is recalling 1,997 units of the Roadrunner PC Hydrophilic Wire Guide due to packaging failure in sterility testing. The device's sterility may be compromised.